Literature DB >> 10606725

Bacillus thuringiensis Cry1Aa toxin-binding region of Bombyx mori aminopeptidase N.

K Yaoi1, K Nakanishi, T Kadotani, M Imamura, N Koizumi, H Iwahana, R Sato.   

Abstract

The Bacillus thuringiensis Cry1Aa toxin-binding region of Bombyx mori aminopeptidase N (APN) was analyzed, to better understand the molecular mechanism of susceptibility to the toxin and the development of resistance in insects. APN was digested with lysylendopeptidase and the ability of the resulting fragments to bind to Cry1Aa and 1Ac toxins was examined. The binding abilities of the two toxins to these fragments were different. The Cry1Aa toxin bound to the fragment containing 40-Asp to 313-Lys, suggesting that the Cry1Aa toxin-binding site is located in the region between 40-Asp and 313-Lys, while Cry1Ac toxin bound exclusively to mature APN. Next, recombinant APN of various lengths was expressed in Escherichia coli cells and its ability to bind to Cry1Aa toxin was examined. The results localized the Cry1Aa toxin binding to the region between 135-Ile and 198-Pro.

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Year:  1999        PMID: 10606725     DOI: 10.1016/s0014-5793(99)01626-9

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  13 in total

1.  A novel aminopeptidase in the fat body of the moth Achaea janata as a receptor for Bacillus thuringiensis Cry toxins and its comparison with midgut aminopeptidase.

Authors:  Madhusudhan Budatha; Gargi Meur; Aparna Dutta-Gupta
Journal:  Biochem J       Date:  2007-07-15       Impact factor: 3.857

Review 2.  Role of receptors in Bacillus thuringiensis crystal toxin activity.

Authors:  Craig R Pigott; David J Ellar
Journal:  Microbiol Mol Biol Rev       Date:  2007-06       Impact factor: 11.056

3.  A 104 kDa Aedes aegypti aminopeptidase N is a putative receptor for the Cry11Aa toxin from Bacillus thuringiensis subsp. israelensis.

Authors:  Jianwu Chen; Supaporn Likitvivatanavong; Karlygash G Aimanova; Sarjeet S Gill
Journal:  Insect Biochem Mol Biol       Date:  2013-10-12       Impact factor: 4.714

4.  Affinity maturation of Cry1Aa toxin to the Bombyx mori cadherin-like receptor by directed evolution.

Authors:  Yuki Fujii; Shiho Tanaka; Manami Otsuki; Yasushi Hoshino; Haruka Endo; Ryoichi Sato
Journal:  Mol Biotechnol       Date:  2013-07       Impact factor: 2.695

5.  Location of the Bombyx mori aminopeptidase N type 1 binding site on Bacillus thuringiensis Cry1Aa toxin.

Authors:  Shogo Atsumi; Eri Mizuno; Hirotaka Hara; Kazuko Nakanishi; Madoka Kitami; Nami Miura; Hiroko Tabunoki; Ayako Watanabe; Ryoichi Sato
Journal:  Appl Environ Microbiol       Date:  2005-07       Impact factor: 4.792

6.  Multiple receptors as targets of Cry toxins in mosquitoes.

Authors:  Supaporn Likitvivatanavong; Jianwu Chen; Amy M Evans; Alejandra Bravo; Mario Soberon; Sarjeet S Gill
Journal:  J Agric Food Chem       Date:  2011-01-06       Impact factor: 5.279

7.  Insecticidal Specificity of Cry1Ah to Helicoverpa armigera Is Determined by Binding of APN1 via Domain II Loops 2 and 3.

Authors:  Zishan Zhou; Yuxiao Liu; Gemei Liang; Yongping Huang; Alejandra Bravo; Mario Soberón; Fuping Song; Xueping Zhou; Jie Zhang
Journal:  Appl Environ Microbiol       Date:  2017-02-01       Impact factor: 4.792

8.  Identification and characterization of Aedes aegypti aminopeptidase N as a putative receptor of Bacillus thuringiensis Cry11A toxin.

Authors:  Jianwu Chen; Karlygash G Aimanova; Songqin Pan; Sarjeet S Gill
Journal:  Insect Biochem Mol Biol       Date:  2009-08-19       Impact factor: 4.714

9.  Binding specificity of Bacillus thuringiensis Cry1Aa for purified, native Bombyx mori aminopeptidase N and cadherin-like receptors.

Authors:  J L Jenkins; D H Dean
Journal:  BMC Biochem       Date:  2001-10-16       Impact factor: 4.059

10.  A genome-wide survey for host response of silkworm, Bombyx mori during pathogen Bacillus bombyseptieus infection.

Authors:  Lulin Huang; Tingcai Cheng; Pingzhen Xu; Daojun Cheng; Ting Fang; Qingyou Xia
Journal:  PLoS One       Date:  2009-12-01       Impact factor: 3.240

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